(Q33750133)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21085648%20AND%20SRC:MED&resulttype=core&format=json

16 January 2020

title

An evolutionary framework for association testing in resequencing studies (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21085648%20AND%20SRC:MED&resulttype=core&format=json

16 January 2020

author

Christopher Ryan King

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21085648%20AND%20SRC:MED&resulttype=core&format=json

16 January 2020

Dan L. Nicolae

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21085648%20AND%20SRC:MED&resulttype=core&format=json

16 January 2020

author name string

Paul J Rathouz

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21085648%20AND%20SRC:MED&resulttype=core&format=json

16 January 2020

publication date

11 November 2010

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21085648%20AND%20SRC:MED&resulttype=core&format=json

16 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21085648%20AND%20SRC:MED&resulttype=core&format=json

16 January 2020

volume

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21085648%20AND%20SRC:MED&resulttype=core&format=json

16 January 2020

issue

11

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21085648%20AND%20SRC:MED&resulttype=core&format=json

16 January 2020

page(s)

e1001202

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21085648%20AND%20SRC:MED&resulttype=core&format=json

Creative Commons Attribution 4.0 International

16 January 2020

copyright license

start time

11 November 2010

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

cites work

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1 reference

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The genetics of human adaptation: hard sweeps, soft sweeps, and polygenic adaptation

21 June 2018

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Evolution in health and medicine Sackler colloquium: Genetic architecture of a complex trait and its implications for fitness and genome-wide association studies

21 June 2018

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Inferring the joint demographic history of multiple populations from multidimensional SNP frequency data

21 June 2018

1 reference

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Finding the missing heritability of complex diseases

21 June 2018

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Evolutionary processes acting on candidate cis-regulatory regions in humans inferred from patterns of polymorphism and divergence

21 June 2018

1 reference

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Parkinson's disease and low frequency alleles found together throughout LRRK2.

21 June 2018

1 reference

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Discovery of rare variants via sequencing: implications for the design of complex trait association studies

21 June 2018

1 reference

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Signals of recent positive selection in a worldwide sample of human populations

21 June 2018

1 reference

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Darwinian and demographic forces affecting human protein coding genes

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2978703

Genetic variation in ANGPTL4 provides insights into protein processing and function

21 June 2018

1 reference

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A highly conserved motif within the NH2-terminal coiled-coil domain of angiopoietin-like protein 4 confers its inhibitory effects on lipoprotein lipase by disrupting the enzyme dimerization.

21 June 2018

1 reference

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A groupwise association test for rare mutations using a weighted sum statistic

21 June 2018

1 reference

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Power of deep, all-exon resequencing for discovery of human trait genes

21 June 2018

1 reference

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Rare loss-of-function mutations in ANGPTL family members contribute to plasma triglyceride levels in humans.

21 June 2018

1 reference

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Personal genomes: The case of the missing heritability

21 June 2018

1 reference

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A flexible forward simulator for populations subject to selection and demography

21 June 2018

1 reference

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Methods for detecting associations with rare variants for common diseases: application to analysis of sequence data

21 June 2018

1 reference

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Simultaneous analysis of all SNPs in genome-wide and re-sequencing association studies

21 June 2018

1 reference

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Assessing the evolutionary impact of amino acid mutations in the human genome

21 June 2018

1 reference

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Data and theory point to mainly additive genetic variance for complex traits

21 June 2018

1 reference

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A powerful and flexible multilocus association test for quantitative traits

21 June 2018

1 reference

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Shifting paradigm of association studies: value of rare single-nucleotide polymorphisms

21 June 2018

1 reference

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The distribution of fitness effects of new mutations

21 June 2018

1 reference

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Medical sequencing at the extremes of human body mass

21 June 2018

1 reference

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Most rare missense alleles are deleterious in humans: implications for complex disease and association studies

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2978703

Population-based resequencing of ANGPTL4 uncovers variations that reduce triglycerides and increase HDL.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2978703

Soft sweeps III: the signature of positive selection from recurrent mutation

21 June 2018

1 reference

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Sequence variations in PCSK9, low LDL, and protection against coronary heart disease

21 June 2018

1 reference

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The distribution of fitness effects of new deleterious amino acid mutations in humans

21 June 2018

1 reference

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A map of recent positive selection in the human genome

21 June 2018

1 reference

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A spectrum of PCSK9 alleles contributes to plasma levels of low-density lipoprotein cholesterol.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2978703

Multiple rare variants in NPC1L1 associated with reduced sterol absorption and plasma low-density lipoprotein levels

21 June 2018

1 reference

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Theoretical models of selection and mutation on quantitative traits

21 June 2018

1 reference

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Association mapping and fine mapping with TreeLD

21 June 2018

1 reference

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Prevalence of hepatic steatosis in an urban population in the United States: impact of ethnicity

21 June 2018

1 reference

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Multiple Rare Alleles Contribute to Low Plasma Levels of HDL Cholesterol

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2978703

The allelic architecture of human disease genes: common disease-common variant... or not?

21 June 2018

1 reference

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MULTIFACTORIAL GENETICSUNDERSTANDING QUANTITATIVE GENETIC VARIATION

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2978703

Are rare variants responsible for susceptibility to complex diseases?

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2978703

The effect of retrospective sampling on binary regression models for clustered data

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2978703

Joint inference of the distribution of fitness effects of deleterious mutations and population demography based on nucleotide polymorphism frequencies

21 June 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1001202

Divergence and polymorphism under the nearly neutral theory of molecular evolution.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1001202

The Dallas Heart Study: a population-based probability sample for the multidisciplinary study of ethnic differences in cardiovascular health.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1001202

A strategy to discover genes that carry multi-allelic or mono-allelic risk for common diseases: a cohort allelic sums test (CAST).

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1001202

Comparisons of site- and haplotype-frequency methods for detecting positive selection.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1001202

Effects of genetic drift on variance components under a general model of epistasis

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21085648

12 December 2020

inferred from PubMed ID database lookup

Distribution of the strength of selection against amino acid replacements in human proteins

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21085648

12 December 2020

inferred from PubMed ID database lookup

Resequencing genomic DNA of patients with severe hypertriglyceridemia (MIM 144650)

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21085648

12 December 2020

inferred from PubMed ID database lookup

Identifiers

DOI

10.1371/JOURNAL.PGEN.1001202

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21085648%20AND%20SRC:MED&resulttype=core&format=json

release_ypwcs6lsxba2lpyfef7hcs3nyi

16 January 2020

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/ypwcs6lsxba2lpyfef7hcs3nyi

24 November 2022

mapped directly with Wikidata item

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21085648%20AND%20SRC:MED&resulttype=core&format=json

16 January 2020

PubMed publication ID

21085648

1 reference